| Childhood obesity PW Speiser, MCJ Rudolf, H Anhalt, C Camacho-Hubner, F Chiarelli, ... The journal of clinical endocrinology & metabolism 90 (3), 1871-1887, 2005 | 1130 | 2005 |
| Child health, developmental plasticity, and epigenetic programming Z Hochberg, R Feil, M Constancia, M Fraga, C Junien, JC Carel, ... Endocrine reviews 32 (2), 159-224, 2011 | 803 | 2011 |
| Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3 B Lorenz-Depiereux, A Benet-Pages, G Eckstein, Y Tenenbaum-Rakover, ... The American Journal of Human Genetics 78 (2), 193-201, 2006 | 401 | 2006 |
| Endocrinology of adipose tissue-an update P Fischer-Posovszky, M Wabitsch, Z Hochberg Hormone and Metabolic Research 39 (05), 314-321, 2007 | 334 | 2007 |
| A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin. PC White, J Dupont, MI New, E Leiberman, Z Hochberg, A Rösler The Journal of clinical investigation 87 (5), 1664-1667, 1991 | 304 | 1991 |
| The use of bone age in clinical practice–part 1 DD Martin, JM Wit, Z Hochberg, L Sävendahl, RR Van Rijn, O Fricke, ... Hormone research in paediatrics 76 (1), 1-9, 2011 | 243 | 2011 |
| Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients L Maimoun, P Philibert, B Cammas, F Audran, P Bouchard, P Fenichel, ... The Journal of Clinical Endocrinology & Metabolism 96 (2), 296-307, 2011 | 236 | 2011 |
| Hypophosphatemia: the common denominator of all rickets D Tiosano, Z Hochberg Journal of bone and mineral metabolism 27, 392-401, 2009 | 227 | 2009 |
| Endocrine withdrawal syndromes Z Hochberg, K Pacak, GP Chrousos Endocrine reviews 24 (4), 523-538, 2003 | 224 | 2003 |
| Maternal hypothyroidism may affect fetal growth and neonatal thyroid function S Blazer, Y Moreh-Waterman, R Miller-Lotan, A Tamir, Z Hochberg Obstetrics & Gynecology 102 (2), 232-241, 2003 | 222 | 2003 |
| The distal axis of growth hormone (GH) in nutritional disorders: GH-binding protein, insulin-like growth factor-I (IGF-I), and IGF-I receptors in obesity and anorexia nervosa Z Hochberg, P Hertz, V Colin, S Ish-Shalom, D Yeshurun, MBH Youdim, ... Metabolism 41 (1), 106-112, 1992 | 216 | 1992 |
| Enhancement of human granulopoiesis in vitro by biosynthetic insulin-like growth factor I/somatomedin C and human growth hormone. S Merchav, I Tatarsky, Z Hochberg The Journal of clinical investigation 81 (3), 791-797, 1988 | 206 | 1988 |
| The molecular basis of hereditary 1, 25-dihydroxyvitamin D3 resistant rickets in seven related families. PJ Malloy, Z Hochberg, D Tiosano, JW Pike, MR Hughes, D Feldman The Journal of clinical investigation 86 (6), 2071-2079, 1990 | 202 | 1990 |
| Increased activation of the alternative “backdoor” pathway in patients with 21-hydroxylase deficiency: evidence from urinary steroid hormone analysis C Kamrath, Z Hochberg, MF Hartmann, T Remer, SA Wudy The Journal of Clinical Endocrinology & Metabolism 97 (3), E367-E375, 2012 | 200 | 2012 |
| Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4 B Coyle, R Coffey, JAL Armour, E Gausden, Z Hochberg, A Grossman, ... Nature genetics 12 (4), 421-423, 1996 | 198 | 1996 |
| Emerging adulthood, a pre-adult life-history stage Z Hochberg, M Konner Frontiers in endocrinology 10, 918, 2020 | 188 | 2020 |
| Mechanisms of steroid impairment of growth Z Hochberg Hormone Research 58 (Suppl. 1), 33-38, 2002 | 175 | 2002 |
| Consensus development for the supplementation of vitamin D in childhood and adolescence Z Hochberg, A Bereket, M Davenport, HA Delemarre-Van De Waal, ... Hormone Research in Paediatrics 58 (1), 39-51, 2002 | 175 | 2002 |
| Rickets in the Middle East: role of environment and genetic predisposition GI Baroncelli, A Bereket, M El Kholy, L Audì, Y Cesur, B Ozkan, M Rashad, ... The Journal of Clinical Endocrinology & Metabolism 93 (5), 1743-1750, 2008 | 167 | 2008 |
| An ochre mutation in the vitamin D receptor gene causes hereditary 1, 25-dihydroxyvitamin D3-resistant rickets in three families. HH Ritchie, MR Hughes, ET Thompson, PJ Malloy, Z Hochberg, ... Proceedings of the National Academy of Sciences 86 (24), 9783-9787, 1989 | 157 | 1989 |
